Testing Overview

The following table summarises the scope of independent testing conducted on Golden Shilajit products.

For a full overview of both documented batches and their laboratory evidence, see the Batch Verification & Laboratory Evidence hub, covering SLJT01LQ and HI-SHL-0226.

Fulvic Acid Analysis

Eurofins Scientific tested the fulvic acid content of Golden Shilajit resin. The result below is specific to batch #SLJT01LQ and is documented in the corresponding Certificate of Analysis. To understand how Eurofins conducts this analysis, see: How Eurofins Tests Shilajit.

45.39 g/100g is the documented result for tested batch #SLJT01LQ. This figure is batch-specific and does not represent a guaranteed minimum or fixed specification for all batches. The fulvic acid analysis (IRXNK method) is marked on the Eurofins report as not ISO accredited; this notation does not apply to the separate ICP-MS heavy-metal analysis.

Heavy Metals Testing

Eurofins Scientific tested Golden Shilajit for the presence of heavy metals using ICP Mass Spectrometry (ICP_MS_S). Results are documented in the Certificate of Analysis for batch #SLJT01LQ. For context, see: Heavy Metals in Shilajit: What Buyers Must Know.

The fulvic acid analysis (IRXNK method) is marked on the Eurofins report as not ISO accredited. The heavy-metal ICP-MS results (ICP_MS_S) are separate from this notation and are not affected by it. <0.00338 mcg/Serving Size for Mercury indicates a result below the method quantification threshold — it does not mean zero. All results are batch-specific to SLJT01LQ only.

Bureau Veritas Microbiological Test Report

Golden Shilajit batch SLJT01LQ was submitted for microbiological analysis by Bureau Veritas. The report includes testing for common microbiological indicators and pathogens.

The same report also includes sensory analysis and additional genetic screening.

Bureau Veritas Test Report — Shilajit, Batch SLJT01LQ, reported 06 May 2026.

How to Read the Reports

A Certificate of Analysis (COA) is a document issued by an accredited laboratory that records the results of testing conducted on a specific product sample. Each COA is tied to a batch number, which identifies the specific production run that was tested.

When reviewing a COA, the batch number confirms which production run the results apply to. Results from one batch are not automatically transferable to another. Golden Shilajit tests each batch independently, and the corresponding COA is specific to that batch.

To confirm that a report applies to your product, match the batch number on your product packaging to the batch number referenced in the laboratory report. For a step-by-step walkthrough, see: How to Read a Shilajit Certificate of Analysis.

Laboratory Report

The Certificate of Analysis below is issued by Eurofins Scientific for batch #SLJT01LQ.

Eurofins Scientific COA — Batch #SLJT01LQ. Fulvic acid and heavy metals analysis.

Our Testing Approach

Each batch of Golden Shilajit is submitted for independent laboratory testing before it is made available for sale. Testing is conducted by accredited third-party laboratories with no commercial interest in the outcome. Results are documented per batch and published here to allow customers to review the specific data relevant to their product.

Batch HI-SHL-0226 — Independent Laboratory Testing

Results below apply only to batch/lot HI-SHL-0226. Different laboratories and methods may report values differently; results must not be averaged or transferred to another batch.

Fulvic Acid & Heavy Metals — Batch HI-SHL-0226

The fulvic acid analysis (IRXNK method) is marked on the Eurofins report as not ISO accredited. The heavy-metal ICP-MS results (ICP_MS_S) are separate from this notation and are not affected by it. <0.00250 mcg/Serving Size for Mercury indicates a result below the method quantification threshold — it does not mean zero. All results are batch-specific to HI-SHL-0226 only.

Heavy Metals by ICP-MS — Batch HI-SHL-0226

Anresco measures total arsenic and does not distinguish organic from inorganic arsenic. Results are reported at a maximum daily intake of 0.5 g. The report states that the sample does not exceed the referenced NSRL/MADL for the other listed heavy metals and would not require a California Prop 65 warning on that basis. ND = Not Detected at the method reporting threshold. All results are batch-specific to HI-SHL-0226 only and must not be compared directly with results from other laboratories using different methods or serving sizes.

Fulvic Acid — ISO 5073:2021 — Batch HI-SHL-0226

This result (44.31%) is a separate laboratory determination by TTI using ISO 5073:2021 and must not be averaged with or compared directly to the Eurofins result (46.80 g/100g) for the same batch. Both results are batch-specific to HI-SHL-0226 only.

Frequently Asked Questions